Rosai Dorfman Testis: A Rare Case ReportNirupma Lal, Parul Gupta, Neema Tiwari*, Sania Zahra Rizvi and Osman Musa
Department Of Pathology, Eras Lucknow Medical College, Lucknow, India
- *Corresponding Author:
- Dr. Neema Tiwari
Department Of Pathology
Eras Lucknow Medical College and Hospital, India
E-mail: [email protected]
Received date: June 07, 2017, Accepted date: June 15, 2017, Published date: June 22, 2017
Citation: Lal N, Gupta P, Tiwari N, Rizvi ZS, Musa O (2017) Rosai Dorfman Testis: A Rare Case Report. J Med Diagn Meth 6:247. doi: 10.4172/2168-9784.1000247
Copyright: © 2017 Nirupma L, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Rosai dorfman disease was defined by Rosai and Dorfman as an idiopathic histiocytic proliferative disorder afflicting nodes in the year 1969. The disease presents in the 10-20 year age group mainly as fever, painless lymphadenopathy, and hypergammaglobulinaemia, however older ages can also be affected. Although it is mainly a node involving disease, 25% extranodal cases have been reported worldwide. The eyes and ocular adnexa, head and neck region upper respiratory tract, skin and subcutaneous tissue, and central nervous system are the commonly involved extranodal sites. We present a case of extranodal testicular Rosai Dorfman in a 40 year old male with right testicular lump which radiologically mimicked a malignancy but on histopathology was diagnosed to be a benign Testicular Rosai Dorfman.